EFFICACY OF A HYDROXYNAPHTHOQUINONE, 566C80, IN EXPERIMENTAL PNEUMOCYSTIS-CARINII PNEUMONITIS

被引:124
作者
HUGHES, WT [1 ]
GRAY, VL [1 ]
GUTTERIDGE, WE [1 ]
LATTER, VS [1 ]
PUDNEY, M [1 ]
机构
[1] WELLCOME RES LABS, BECKENHAM BR3 3BS, KENT, ENGLAND
关键词
D O I
10.1128/AAC.34.2.225
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The efficacy of a new class of drugs for Pneumocystis carinii pneumonitis was demonstrated. 566C80, a hydroxynaphthoquinone, administered orally in a dose of ≥ 100 mg/kg of body weight per day prophylactically prevented P. carinii pneumonitis in 90% or more of rats, while all untreated control animals developed pneumonitis. When 566C80 (100 mg/kg per day) was administered for 3 weeks after P. carinii pneumonitis was established, therapy was totally effective and all of the untreated controls had progressive P. carinii pneumonitis. A dose of 566C80 of between 25 and 50 mg/kg per day protected 50% of the rats from P. carinii pneumonitis, and a dose of between 50 and 100 mg/kg per day cured 50% of those treated for P. carinii pneumonitis. Both prophylaxis and treatment with 566C80 were at least as effective as with trimethoprim-sulfamethoxazole. Animals maintained on immunosuppression after completion of treatment remained free of P. carinii, suggesting a killing effect. Clearance of P. carinii was associated with levels of 60 μg or more of 556C80 per ml of plasma. This hydroxynaphthoquinone offers promise as an anti-P. carinii drug.
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页码:225 / 228
页数:4
相关论文
共 13 条
[1]   SUPEROXIDE ANION PRODUCTION AND TRYPANOCIDAL ACTION OF NAPHTHOQUINONES ON TRYPANOSOMA-CRUZI [J].
BOVERIS, A ;
STOPPANI, AOM ;
DOCAMPO, R ;
CRUZ, FS .
COMPARATIVE BIOCHEMISTRY AND PHYSIOLOGY C-PHARMACOLOGY TOXICOLOGY & ENDOCRINOLOGY, 1978, 61 (02) :327-329
[2]   LIPID PEROXIDATION AND GENERATION OF FREE-RADICALS, SUPEROXIDE ANION, AND HYDROGEN-PEROXIDE IN BETA-LAPACHONE-TREATED TRYPANOSOMA-CRUZI EPIMASTIGOTES [J].
DOCAMPO, R ;
CRUZ, FS ;
BOVERIS, A ;
MUNIZ, RPA ;
ESQUIVEL, DMS .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1978, 186 (02) :292-297
[3]   NAPHTHOQUINONE ANTIMALARIALS .29. 2-HYDROXY-3-(OMEGA-CYCLOHEXYLALKYL)-1,4-NAPHTHOQUINONES [J].
FIESER, LF ;
SCHIRMER, JP ;
ARCHER, S ;
LORENZ, RR ;
PFAFFENB.PI .
JOURNAL OF MEDICINAL CHEMISTRY, 1967, 10 (04) :513-+
[4]   POTENT AND SELECTIVE HYDROXYNAPHTHOQUINONE INHIBITORS OF MITOCHONDRIAL ELECTRON-TRANSPORT IN EIMERIA-TENELLA (APICOMPLEXA, COCCIDIA) [J].
FRY, M ;
HUDSON, AT ;
RANDALL, AW ;
WILLIAMS, RB .
BIOCHEMICAL PHARMACOLOGY, 1984, 33 (13) :2115-2122
[5]   NOVEL ANTI-MALARIAL HYDROXYNAPHTHOQUINONES WITH POTENT BROAD-SPECTRUM ANTI-PROTOZOAL ACTIVITY [J].
HUDSON, AT ;
RANDALL, AW ;
FRY, M ;
GINGER, CD ;
HILL, B ;
LATTER, VS ;
MCHARDY, N ;
WILLIAMS, RB .
PARASITOLOGY, 1985, 90 (FEB) :45-55
[6]  
HUDSON AT, 1988, TOPICS MED CHEM SPEC, V65, P266
[7]   SUCCESSFUL CHEMOPROPHYLAXIS FOR PNEUMOCYSTIS-CARINII PNEUMONITIS [J].
HUGHES, WT ;
KUHN, S ;
CHAUDHARY, S ;
FELDMAN, S ;
VERZOSA, M ;
AUR, RJA ;
PRATT, C ;
GEORGE, SL .
NEW ENGLAND JOURNAL OF MEDICINE, 1977, 297 (26) :1419-1426
[8]  
HUGHES WT, 1979, ANTIMICROB AGENTS CH, V16, P333, DOI 10.1128/AAC.16.3.333
[9]   EFFICACY OF TRIMETHOPRIM AND SULFAMETHOXAZOLE IN PREVENTION AND TREATMENT OF PNEUMOCYSTIS-CARINII PNEUMONITIS [J].
HUGHES, WT ;
MCNABB, PC ;
MAKRES, TD ;
FELDMAN, S .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1974, 5 (03) :289-293
[10]   INVITRO AND INVIVO EVALUATION OF TOXICITY OF 1,4-NAPHTHOQUINONE AND 1,2-NAPHTHOQUINONE DERIVATIVES AGAINST TRYPANOSOMA-CRUZI [J].
LOPES, JN ;
CRUZ, FS ;
DOCAMPO, R ;
VASCONCELLOS, ME ;
SAMPAIO, MCR ;
PINTO, AV ;
GILBERT, B .
ANNALS OF TROPICAL MEDICINE AND PARASITOLOGY, 1978, 72 (06) :523-531